A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581012



Internal ID16368421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062091..13148893hg38UCSC Ensembl
Innerchr2:13202216..13289018hg19UCSC Ensembl
Innerchr2:13119667..13206469hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3886803
hg1986803
hg1886803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n54
Supporting Variantsnssv1150402
SamplesNINDS_222
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581012
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer